Nielsen FC - Search Results

1

Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndrome.

Ou J, Rasmussen M, Westers H, Andersen SD, Jager PO, Kooi KA, Niessen RC, Eggen BJ, Nielsen FC, Kleibeuker JH, Sijmons RH, Rasmussen LJ, Hofstra RM. Ou J, et al. Among authors: nielsen fc. Genes Chromosomes Cancer. 2009 Apr;48(4):340-50. doi: 10.1002/gcc.20644. Genes Chromosomes Cancer. 2009. PMID: 19156873 Free article.

2

Functional characterization of MLH1 missense variants identified in Lynch syndrome patients.

Andersen SD, Liberti SE, Lützen A, Drost M, Bernstein I, Nilbert M, Dominguez M, Nyström M, Hansen TV, Christoffersen JW, Jäger AC, de Wind N, Nielsen FC, Tørring PM, Rasmussen LJ. Andersen SD, et al. Among authors: nielsen fc. Hum Mutat. 2012 Dec;33(12):1647-55. doi: 10.1002/humu.22153. Epub 2012 Jul 23. Hum Mutat. 2012. PMID: 22753075

3

Genetic screens to identify pathogenic gene variants in the common cancer predisposition Lynch syndrome.

Drost M, Lützen A, van Hees S, Ferreira D, Calléja F, Zonneveld JB, Nielsen FC, Rasmussen LJ, de Wind N. Drost M, et al. Among authors: nielsen fc. Proc Natl Acad Sci U S A. 2013 Jun 4;110(23):9403-8. doi: 10.1073/pnas.1220537110. Epub 2013 May 20. Proc Natl Acad Sci U S A. 2013. PMID: 23690608 Free PMC article.

4

Nuclear localization of human DNA mismatch repair protein exonuclease 1 (hEXO1).

Knudsen NØ, Nielsen FC, Vinther L, Bertelsen R, Holten-Andersen S, Liberti SE, Hofstra R, Kooi K, Rasmussen LJ. Knudsen NØ, et al. Among authors: nielsen fc. Nucleic Acids Res. 2007;35(8):2609-19. doi: 10.1093/nar/gkl1166. Epub 2007 Apr 10. Nucleic Acids Res. 2007. PMID: 17426132 Free PMC article.

5

Functional analysis of HNPCC-related missense mutations in MSH2.

Lützen A, de Wind N, Georgijevic D, Nielsen FC, Rasmussen LJ. Lützen A, et al. Among authors: nielsen fc. Mutat Res. 2008 Oct 14;645(1-2):44-55. doi: 10.1016/j.mrfmmm.2008.08.015. Epub 2008 Sep 4. Mutat Res. 2008. PMID: 18822302

6

HNPCC mutations in the human DNA mismatch repair gene hMLH1 influence assembly of hMutLalpha and hMLH1-hEXO1 complexes.

Jäger AC, Rasmussen M, Bisgaard HC, Singh KK, Nielsen FC, Rasmussen LJ. Jäger AC, et al. Among authors: nielsen fc. Oncogene. 2001 Jun 14;20(27):3590-5. doi: 10.1038/sj.onc.1204467. Oncogene. 2001. PMID: 11429708

7

Nuclear translocation contributes to regulation of DNA excision repair activities.

Knudsen NØ, Andersen SD, Lützen A, Nielsen FC, Rasmussen LJ. Knudsen NØ, et al. Among authors: nielsen fc. DNA Repair (Amst). 2009 Jun 4;8(6):682-9. doi: 10.1016/j.dnarep.2009.03.005. Epub 2009 Apr 18. DNA Repair (Amst). 2009. PMID: 19376751 Review.

8

Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patients.

Petersen SM, Dandanell M, Rasmussen LJ, Gerdes AM, Krogh LN, Bernstein I, Okkels H, Wikman F, Nielsen FC, Hansen TV. Petersen SM, et al. Among authors: nielsen fc. BMC Med Genet. 2013 Oct 3;14:103. doi: 10.1186/1471-2350-14-103. BMC Med Genet. 2013. PMID: 24090359 Free PMC article.

9

Bi-directional routing of DNA mismatch repair protein human exonuclease 1 to replication foci and DNA double strand breaks.

Liberti SE, Andersen SD, Wang J, May A, Miron S, Perderiset M, Keijzers G, Nielsen FC, Charbonnier JB, Bohr VA, Rasmussen LJ. Liberti SE, et al. Among authors: nielsen fc. DNA Repair (Amst). 2011 Jan 2;10(1):73-86. doi: 10.1016/j.dnarep.2010.09.023. Epub 2010 Oct 20. DNA Repair (Amst). 2011. PMID: 20970388 Free PMC article.

10

Identification of factors interacting with hMSH2 in the fetal liver utilizing the yeast two-hybrid system. In vivo interaction through the C-terminal domains of hEXO1 and hMSH2 and comparative expression analysis.

Rasmussen LJ, Rasmussen M, Lee B, Rasmussen AK, Wilson DM 3rd, Nielsen FC, Bisgaard HC. Rasmussen LJ, et al. Among authors: nielsen fc. Mutat Res. 2000 Jun 30;460(1):41-52. doi: 10.1016/s0921-8777(00)00012-4. Mutat Res. 2000. PMID: 10856833

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